US5332828A - Process for the preparation of bis (2-benzoxazolyl) stilbenes - Google Patents
Process for the preparation of bis (2-benzoxazolyl) stilbenes Download PDFInfo
- Publication number
- US5332828A US5332828A US08/020,914 US2091493A US5332828A US 5332828 A US5332828 A US 5332828A US 2091493 A US2091493 A US 2091493A US 5332828 A US5332828 A US 5332828A
- Authority
- US
- United States
- Prior art keywords
- benzoxazolyl
- bis
- carbon atoms
- compounds
- preparation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 14
- 238000002360 preparation method Methods 0.000 title claims abstract description 8
- -1 2-benzoxazolyl Chemical group 0.000 title claims description 6
- 150000001629 stilbenes Chemical class 0.000 title 1
- 235000021286 stilbenes Nutrition 0.000 title 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims abstract description 12
- SBBQDUFLZGOASY-OWOJBTEDSA-N 4-[(e)-2-(4-carboxyphenyl)ethenyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1\C=C\C1=CC=C(C(O)=O)C=C1 SBBQDUFLZGOASY-OWOJBTEDSA-N 0.000 claims abstract description 12
- ORACIQIJMCYPHQ-MDZDMXLPSA-N 2-[4-[(e)-2-[4-(1,3-benzoxazol-2-yl)phenyl]ethenyl]phenyl]-1,3-benzoxazole Chemical class C1=CC=C2OC(C3=CC=C(C=C3)/C=C/C=3C=CC(=CC=3)C=3OC4=CC=CC=C4N=3)=NC2=C1 ORACIQIJMCYPHQ-MDZDMXLPSA-N 0.000 claims abstract description 10
- 239000003054 catalyst Substances 0.000 claims abstract description 10
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 10
- 239000010936 titanium Substances 0.000 claims abstract description 10
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 150000002790 naphthalenes Chemical class 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 238000009835 boiling Methods 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 239000002904 solvent Substances 0.000 abstract description 8
- 238000006243 chemical reaction Methods 0.000 abstract description 4
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000012320 chlorinating reagent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- SVNDCMCAPDWHPV-UHFFFAOYSA-N 2-[2-(1,3-benzoxazol-2-yl)-1,2-diphenylethenyl]-1,3-benzoxazole Chemical class C1=CC=CC=C1C(C=1OC2=CC=CC=C2N=1)=C(C=1C=CC=CC=1)C1=NC2=CC=CC=C2O1 SVNDCMCAPDWHPV-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical class C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 1
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
- BSZXAFXFTLXUFV-UHFFFAOYSA-N 1-phenylethylbenzene Chemical compound C=1C=CC=CC=1C(C)C1=CC=CC=C1 BSZXAFXFTLXUFV-UHFFFAOYSA-N 0.000 description 1
- RPJUVNYXHUCRMG-UHFFFAOYSA-N 2-amino-4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(N)=C1 RPJUVNYXHUCRMG-UHFFFAOYSA-N 0.000 description 1
- OKEZAUMKBWTTCR-AATRIKPKSA-N 5-methyl-2-[4-[(e)-2-[4-(5-methyl-1,3-benzoxazol-2-yl)phenyl]ethenyl]phenyl]-1,3-benzoxazole Chemical compound CC1=CC=C2OC(C3=CC=C(C=C3)/C=C/C3=CC=C(C=C3)C=3OC4=CC=C(C=C4N=3)C)=NC2=C1 OKEZAUMKBWTTCR-AATRIKPKSA-N 0.000 description 1
- PSVDQOKAQPGOLT-UHFFFAOYSA-N 5-tert-butyl-2-[4-[2-[4-(5-tert-butyl-1,3-benzoxazol-2-yl)phenyl]ethenyl]phenyl]-1,3-benzoxazole Chemical compound CC(C)(C)C1=CC=C2OC(C3=CC=C(C=C3)C=CC3=CC=C(C=C3)C=3OC4=CC=C(C=C4N=3)C(C)(C)C)=NC2=C1 PSVDQOKAQPGOLT-UHFFFAOYSA-N 0.000 description 1
- AFTULNXJGJGVRY-UHFFFAOYSA-N CC(C)[O-].CC(C)[O-].CC(C)[O-].CC([Ti+3])=O Chemical compound CC(C)[O-].CC(C)[O-].CC(C)[O-].CC([Ti+3])=O AFTULNXJGJGVRY-UHFFFAOYSA-N 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- 238000006136 alcoholysis reaction Methods 0.000 description 1
- 150000008378 aryl ethers Chemical class 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D263/57—Aryl or substituted aryl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/62—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems having two or more ring systems containing condensed 1,3-oxazole rings
- C07D263/64—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems having two or more ring systems containing condensed 1,3-oxazole rings linked in positions 2 and 2' by chains containing six-membered aromatic rings or ring systems containing such rings
Definitions
- This invention pertains to the preparation of 4,4'-bis(2-benzoxazolyl)stilbene compounds by the reaction of 4,4'-stilbenedicarboxylic acid with 2-aminophenol compounds in the presence of a tin or titanium catalyst and certain solvents.
- Unsubstituted and substituted 4,4'-bis(2-benzoxazolyl)stilbene compounds are known compositions of matter which are useful as optical brightening or whitening agents in various polymeric materials, particularly fiber-forming, synthetic polymers.
- U.S. Pat. No. 4,921,964 discloses the preparation of bis(2-benzoxazolyl)stilbene compounds by the reaction of dialkyl stilbenedicarboxylate ester with various 2-aminophenol compounds in the presence of certain solvents and catalysts.
- 4,4'-stilbenedicarboxylic acid in preparing 4,4'-bis(2-benzoxazolyl)stilbene compounds generally does not give satisfactory results because of the high melting point of the diacid and its limited solubility in many solvents.
- the '089 patent discloses that 4,4'-stilbenedicarboxylic acid may be used in the preparation of 4,4'-bis(2-benzoxazolyl)stilbene compounds by the reaction thereof with certain 2-aminophenols using a substantial amount of powerful phosphoric acid dehydrating agents such as pyrophosphoric and polyphosphoric acids as the reaction medium.
- 4,4'-bis(2-benzoxazolyl)stilbene compounds may be obtained in good purity and yields by a simple, one-step process wherein 4,4'-stilbenedicarboxylic acid is reacted with 2-aminophenol compounds in the presence of a tin or titanium catalyst and certain solvents.
- the present invention therefore provides a process for the preparation of 4,4'-bis(2-benzoxazolyl)stilbene compounds having the formula ##STR1## which comprises reacting 4,4'-stilbenedicarboxylic acid with one or more 2-aminophenol compounds having the formula ##STR2## in the presence of a tin or titanium catalyst and an inert organic solvent having a boiling point above 200° C., wherein each R 1 is independently selected from hydrogen, alkyl of up to about 12 carbon atoms and alkoxy of up to about 12 carbon atoms. R 1 preferably represents hydrogen or alkyl of up to about 4 carbon atoms, especially methyl.
- the 4,4'-bis(2-benzoxazolyl)stilbene products may be isolated by filtration in a purity which is sufficient for use without further purification.
- inert, organic solvents examples include naphthalene; alkyl-substituted naphthalene compounds such as methylnaphthalene and dimethylnaphthalenes; halogenated naphthalenes such as chloronaphthalene; biphenyl; aromatic ethers such as diphenylether; aromatic alkanes such as diphenylethane; and the like.
- Alkyl-substituted naphthalenes containing a total of 11 to 20 carbon atoms represent the preferred solvents.
- the amount of solvent employed is not important. However, the weight ratio of the solvent to the total weight of the 4,4'-stilbenedicarboxylic acid with 2-aminophenol reactants typically will be in the range of 2:1 to 10:1.
- the process typically is carried out over a temperature range of about 200° to 300° C., preferably 220° to 260° C.
- Pressure normally is not an important process condition and the process therefore normally is performed at ambient pressure or moderately elevated pressure generated in a sealed reactor, i.e., autogenous pressures.
- the organo-tin and organo-titanium catalyst compounds useful in my novel process are well known esterification, polyesterification, alcoholysis, and acidolysis catalysts. These compounds are described in U.S. Pat. No. 3,585,208 and references cited therein.
- the prepared organo-titanium compounds are titanium alkoxides containing a total of up 20 carbon atoms. preferably 4 to 16 carbon atoms. Titanium tetraisopropoxide and acetyltitanium triisopropoxide are specific examples of suitable organo-titanium catalysts.
- the organo tin compounds may be selected from dihydrocarbyltin oxides such as dibutyltin oxide.
- the amount of the organo-titanium and organo-tin catalysts which may be used normally is in the range of about 5 to 20 mole percent based on the moles of 4,4'-stilbenedicarboxylic acid present.
- Example 1 The procedure of Example 1 was repeated using equimolar amounts of 2-amine-4-methylphenol and 2-amino-4-tertiary butylphenol to obtain 4,4'-bis(5-methyl-2-benzoxazolyl)stilbene and 4,4'-bis(5-t-butyl-2-benzoxazolyl)stilbene in yields of 90 to 95%.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/020,914 US5332828A (en) | 1993-02-22 | 1993-02-22 | Process for the preparation of bis (2-benzoxazolyl) stilbenes |
| DK94910157.0T DK0684946T3 (el) | 1993-02-22 | 1994-02-14 | |
| AT94910157T ATE152105T1 (de) | 1993-02-22 | 1994-02-14 | Verfahren zur herstellung von bis(2- benzoxazolyl)stilbenen |
| EP94910157A EP0684946B1 (en) | 1993-02-22 | 1994-02-14 | Process for the preparation of bis(2-benzoxazolyl)stilbenes |
| JP6519242A JPH08507074A (ja) | 1993-02-22 | 1994-02-14 | ビス（２−ベンゾオキサゾリル）スチルベンの製造方法 |
| KR1019950703454A KR960701027A (ko) | 1993-02-22 | 1994-02-14 | 비스(2-벤족사졸릴)스틸벤의 제조 방법(process for the preparation of bis(2-benzoxazolyl) stilbenes) |
| CA002153796A CA2153796A1 (en) | 1993-02-22 | 1994-02-14 | Process for the preparation of bis(2-benzoxazolyl) stilbenes |
| PCT/US1994/001928 WO1994019333A1 (en) | 1993-02-22 | 1994-02-14 | Process for the preparation of bis(2-benzoxazolyl)stilbenes |
| ES94910157T ES2102847T3 (es) | 1993-02-22 | 1994-02-14 | Procedimiento para la preparacion de bis(2-benzoxazolil)estilbenos. |
| DE69402832T DE69402832T2 (de) | 1993-02-22 | 1994-02-14 | Verfahren zur herstellung von bis(2-benzoxazolyl)stilbenen |
| GR970401208T GR3023557T3 (en) | 1993-02-22 | 1997-05-26 | Process for the preparation of bis(2-benzoxazolyl)stilbenes. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/020,914 US5332828A (en) | 1993-02-22 | 1993-02-22 | Process for the preparation of bis (2-benzoxazolyl) stilbenes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5332828A true US5332828A (en) | 1994-07-26 |
Family
ID=21801261
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/020,914 Expired - Lifetime US5332828A (en) | 1993-02-22 | 1993-02-22 | Process for the preparation of bis (2-benzoxazolyl) stilbenes |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5332828A (el) |
| EP (1) | EP0684946B1 (el) |
| JP (1) | JPH08507074A (el) |
| KR (1) | KR960701027A (el) |
| AT (1) | ATE152105T1 (el) |
| CA (1) | CA2153796A1 (el) |
| DE (1) | DE69402832T2 (el) |
| DK (1) | DK0684946T3 (el) |
| ES (1) | ES2102847T3 (el) |
| GR (1) | GR3023557T3 (el) |
| WO (1) | WO1994019333A1 (el) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6177574B1 (en) | 2000-03-02 | 2001-01-23 | Eastman Chemical Company | Preparation of mixtures of benzoxazolyl-stilbene compounds |
| US6565987B2 (en) | 1999-11-12 | 2003-05-20 | Eastman Chemical Company | Non-exuding optically brightened polyolefin blends |
| CZ301894B6 (cs) * | 2000-10-18 | 2010-07-21 | Ciba Specialty Chemicals Holding Inc. | Zpusob prípravy bis-benzazolylových sloucenin |
| CN102070551A (zh) * | 2010-12-29 | 2011-05-25 | 河北星宇化工有限公司 | 2,2-(4,4-二苯乙烯基)双苯并噁唑的制备方法 |
| WO2023128885A1 (en) * | 2021-12-28 | 2023-07-06 | Akdeniz Chemson Kimya Sanayi Ve Ticaret Anonim Sirketi | A synthesis method of benzoxazole based optical brighteners |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3366575A (en) * | 1964-03-13 | 1968-01-30 | Nippon Kayaku Kk | Enhancement of optical brightening effects by using two or more species of brightening agent |
| US3412089A (en) * | 1963-09-18 | 1968-11-19 | Sumitomo Chemical Co | Manufacture of 4, 4'-dibenzoxazol-2-yl stilbene |
| US3585208A (en) * | 1968-08-01 | 1971-06-15 | Eastman Kodak Co | Manufacture of benzoxazoles |
| US3586673A (en) * | 1968-02-05 | 1971-06-22 | Eastman Kodak Co | Preparation of symmetrically and unsymmetrically substituted stilbenebisbenzoxazoles |
| US3768042A (en) * | 1972-06-07 | 1973-10-23 | Motorola Inc | Dielectric cavity stripline coupler |
| US4048185A (en) * | 1975-06-12 | 1977-09-13 | Hoechst Atiengesellschaft | Benzoxazole derivatives, process for their preparation and their use as optical brighteners |
| US4282355A (en) * | 1980-02-14 | 1981-08-04 | Hoechst Aktiengesellschaft | Process for the manufacture of bis-benzoxazolyl-stilbene compounds |
| US4291964A (en) * | 1980-01-28 | 1981-09-29 | Polaroid Corporation | Strobe switch with camera control feature |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1411999A (fr) * | 1964-09-18 | 1965-09-24 | Sumitomo Chemical Co | Procédé de fabrication d'agents de blanchiment optiques |
| US4921964A (en) * | 1989-03-01 | 1990-05-01 | Eastman Kodak Company | Process for the preparation of stilbene derivatives |
-
1993
- 1993-02-22 US US08/020,914 patent/US5332828A/en not_active Expired - Lifetime
-
1994
- 1994-02-14 WO PCT/US1994/001928 patent/WO1994019333A1/en active IP Right Grant
- 1994-02-14 DK DK94910157.0T patent/DK0684946T3/da active
- 1994-02-14 KR KR1019950703454A patent/KR960701027A/ko not_active Application Discontinuation
- 1994-02-14 DE DE69402832T patent/DE69402832T2/de not_active Expired - Fee Related
- 1994-02-14 JP JP6519242A patent/JPH08507074A/ja not_active Ceased
- 1994-02-14 EP EP94910157A patent/EP0684946B1/en not_active Expired - Lifetime
- 1994-02-14 ES ES94910157T patent/ES2102847T3/es not_active Expired - Lifetime
- 1994-02-14 AT AT94910157T patent/ATE152105T1/de not_active IP Right Cessation
- 1994-02-14 CA CA002153796A patent/CA2153796A1/en not_active Abandoned
-
1997
- 1997-05-26 GR GR970401208T patent/GR3023557T3/el unknown
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3412089A (en) * | 1963-09-18 | 1968-11-19 | Sumitomo Chemical Co | Manufacture of 4, 4'-dibenzoxazol-2-yl stilbene |
| US3366575A (en) * | 1964-03-13 | 1968-01-30 | Nippon Kayaku Kk | Enhancement of optical brightening effects by using two or more species of brightening agent |
| US3586673A (en) * | 1968-02-05 | 1971-06-22 | Eastman Kodak Co | Preparation of symmetrically and unsymmetrically substituted stilbenebisbenzoxazoles |
| US3585208A (en) * | 1968-08-01 | 1971-06-15 | Eastman Kodak Co | Manufacture of benzoxazoles |
| US3768042A (en) * | 1972-06-07 | 1973-10-23 | Motorola Inc | Dielectric cavity stripline coupler |
| US4048185A (en) * | 1975-06-12 | 1977-09-13 | Hoechst Atiengesellschaft | Benzoxazole derivatives, process for their preparation and their use as optical brighteners |
| US4291964A (en) * | 1980-01-28 | 1981-09-29 | Polaroid Corporation | Strobe switch with camera control feature |
| US4282355A (en) * | 1980-02-14 | 1981-08-04 | Hoechst Aktiengesellschaft | Process for the manufacture of bis-benzoxazolyl-stilbene compounds |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6565987B2 (en) | 1999-11-12 | 2003-05-20 | Eastman Chemical Company | Non-exuding optically brightened polyolefin blends |
| US6177574B1 (en) | 2000-03-02 | 2001-01-23 | Eastman Chemical Company | Preparation of mixtures of benzoxazolyl-stilbene compounds |
| CZ301894B6 (cs) * | 2000-10-18 | 2010-07-21 | Ciba Specialty Chemicals Holding Inc. | Zpusob prípravy bis-benzazolylových sloucenin |
| CN102070551A (zh) * | 2010-12-29 | 2011-05-25 | 河北星宇化工有限公司 | 2,2-(4,4-二苯乙烯基)双苯并噁唑的制备方法 |
| CN102070551B (zh) * | 2010-12-29 | 2012-06-20 | 河北星宇化工有限公司 | 2,2’-(4,4’-二苯乙烯基)双苯并噁唑的制备方法 |
| WO2023128885A1 (en) * | 2021-12-28 | 2023-07-06 | Akdeniz Chemson Kimya Sanayi Ve Ticaret Anonim Sirketi | A synthesis method of benzoxazole based optical brighteners |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69402832D1 (de) | 1997-05-28 |
| ES2102847T3 (es) | 1997-08-01 |
| WO1994019333A1 (en) | 1994-09-01 |
| ATE152105T1 (de) | 1997-05-15 |
| CA2153796A1 (en) | 1994-09-01 |
| EP0684946A1 (en) | 1995-12-06 |
| JPH08507074A (ja) | 1996-07-30 |
| EP0684946B1 (en) | 1997-04-23 |
| GR3023557T3 (en) | 1997-08-29 |
| DE69402832T2 (de) | 1997-07-31 |
| KR960701027A (ko) | 1996-02-24 |
| DK0684946T3 (el) | 1997-05-26 |
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